"61919-781-90" National Drug Code (NDC)

NDC Code	61919-781-90
Package Description	90 TABLET in 1 BOTTLE (61919-781-90)
Product NDC	61919-781
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20190114
Marketing Category Name	ANDA
Application Number	ANDA200044
Manufacturer	Direct_Rx
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	30
Strength Unit	mg/1
Pharmacy Classes	PPAR alpha [CS], PPAR gamma [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor Activity [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS]